Patent Application
20230249133
This disclosure relates generally to a method and apparatus for electrochemically regenerating hydroxide and carbon dioxide from alkali metal carbonate, and its application to the capture of carbon dioxide directly from the atmosphere.
The accumulation of carbon dioxide (CO2) in the atmosphere is an existential threat to life on Earth.
In the (likely) event that regulation and action fail to limit emissions from combustion of fossil fuel, the viability of civilization may depend on removing CO2 directly from the atmosphere. This improbable engineering task is now being considered for application in the future.
Removal of carbon dioxide (CO2) from the air (known as “Direct Air Capture” or “DAC”) is currently viewed as a potential tool to curb the global warming caused by accumulation of CO2 in Earth's atmosphere. DAC is a known process with several proposed methods. In typical DAC operations, ambient air is contacted with a chemical media such as an aqueous alkaline solvent or functionalized sorbent. One method of DAC under development involves a system wherein CO2 is absorbed from the air to form an aqueous alkaline carbonate solution (Reaction 1) and subsequently recovered by the circuitous closed-loop thermochemical process summarized in Reactions 2, 3, 4:
Wherein, M=alkali metal=lithium (Li), sodium (Na), potassium (K), caesium (Cs) or rubidium (Rb).
The CO2 product from Reaction 3 may be disposed “as is” or preferably converted to useful materials for sale. These options are known respectively as carbon capture and storage (CC&S) and carbon capture and conversion (CC&C). In the latter case the CO2 may be combined with hydrogen by established methods to make fuels, or reduced to various products in electrochemical processes now under development [for example as disclosed in U.S. Pat. No. 4,197,421A and US 2019/0359894A].
The DAC process of Reactions 1-4 has been demonstrated on pilot scale with potassium hydroxide (KOH) absorbent and is considered feasible for large scale development [for example, as disclosed in WO2009155539A3]. However, coupling the fluid absorption with the solid-fluid causticizing system constrains optimization of the DAC process and its broad application is limited by the need to handle hot solids in large equipment not amenable to downscaling.
It is recognized that the DAC system could be simplified and more readily scaled down if the solid dependent regeneration of alkaline absorbent were replaced by a process treating only liquids and gases. Electrochemical methods have been investigated for this role but so far cannot be seen as useful alternatives to the established thermochemical route of Equations 2,3,4. These electrochemical methods essentially involve splitting an alkali metal carbonate (e.g. K2CO3) to give hydroxide (KOH) and carbon dioxide (CO2) with the net result of Reaction 5.
M2CO3(aq)+H2O(l)-2F→2MOH(aq)+CO2(g) Reaction 5
Wherein F=Faraday's number=96489 Coulomb per mole
The attraction of this method is that it could regenerate the absorbent (MOH) and produce CO2 in a single step with only liquid and gas reactants/products at near ambient pressure and temperature. As usual in such cases it is easier to write Reaction 5 than to carry it out in reality with practical results. Nonetheless it remains a desirable goal to replace the thermochemical regeneration of absorbent in DAC with such an electrochemical process.
A primary objective of the present invention is to provide an electrochemical reactor and process to relax/remove the carbonate conversion causticizing constraint imposed by the thermochemical regeneration process in applications such as DAC, while optionally providing for the co-generation of hydrogen and integrated reduction of CO2 to fuels.
According to one aspect of the invention, there is provided an electrochemical reactor for regenerating an alkali metal hydroxide (MOH) and carbon dioxide (CO2) from an alkali metal carbonate (M2CO3) when coupled to a power supply. The electrochemical reactor comprises a porous electronically conductive cathode, a porous electronically insulating hydrophilic transport barrier, a porous electronically conductive hydrophilic anode, a porous hydrophobic gas separation barrier, and a product gas exit channel. The porous electronically conductive cathode has an inlet for receiving a pressurized electrolyte feed stream comprising MOH, M2CO3 and H2O, and an outlet for discharging an electrolyte product stream comprising MOH, M2CO3, H2O and H2. The porous electronically insulating hydrophilic transport barrier is in adjacent contact with the cathode and is configured to regulate the transport of electrolyte species and impede gas flow across the transport barrier. The porous electronically conductive hydrophilic anode is in adjacent contact with the transport barrier and is configured to generate CO2 in the presence of MOH while suppressing their recombination. The porous hydrophobic gas separation barrier is in adjacent contact with the anode and is configured to pass gases including CO2 and suppress liquids. The product gas exit channel is in adjacent contact with the gas separation barrier and serves to discharge an anode product stream comprising at least CO2 gas.
According to another aspect of the invention, there is provided an electrochemical reactor for regenerating MOH and CO2 from M2CO3 when coupled to a power supply. The electrochemical reactor comprises an electrolyte flow channel, a porous electronically insulating hydrophilic first transport barrier, a porous electronically conductive hydrophilic cathode, a porous hydrophobic H2 separation barrier, a cathode gas exit channel, a porous electronically insulating hydrophilic second transport barrier, a porous electronically conductive hydrophilic anode, a porous hydrophobic gas separation barrier, and an anode gas exit channel. The electrolyte flow channel has an inlet for receiving an electrolyte feed stream comprising MOH, M2CO3 and H2O, and an outlet for discharging an electrolyte product stream comprising MOH, M2CO3, and H2O. The porous electronically insulating hydrophilic first transport barrier is in adjacent contact with a first side of the electrolyte flow channel and is configured to regulate the transport of electrolyte species and impede gas flow across the first transport barrier. The porous electronically conductive hydrophilic cathode is in adjacent contact with the first transport barrier. The porous hydrophobic H2 separation barrier is in adjacent contact with the cathode and is configured to pass gases including H2 and suppress liquids. The cathode gas exit channel is in adjacent contact with the H2 separation barrier and serves to discharge a cathode gas stream comprising H2. The porous electronically insulating hydrophilic second transport barrier is in adjacent contact with a second side of the electrolyte flow channel and is configured to regulate the transport of electrolyte species and impede gas flow across the second transport barrier. The porous electronically conductive hydrophilic anode is in adjacent contact with the second transport barrier and is configured to generate CO2 in the presence of MOH while suppressing their recombination. The porous hydrophobic gas separation barrier is in adjacent contact with the anode and is configured to pass gases including CO2 and suppress liquids. The anode gas exit channel is in adjacent contact with the gas separation barrier and serves to discharge an anode product stream comprising at least CO2.
The anode can comprise a biphilic morphology having heterogeneous surfaces with spatially distinct regions of wettability including hydrophilic components. More particularly, the anode can be a biphilic anode comprising multiple porous hydrophilic electrode portions separated by multiple hydrophobic gas disengagement channels and stacked parallel to a direction of electric current in the electrochemical reactor.
The anode can have a porosity from 10 to 90%, a pore size from 10 to 1000 micron, a thickness in direction of current from 0.2 to 20 mm, an air/water wetting angle from 0 to 89° and an air/water capillary pressure at or above 1 kPa. The gas separation barrier can have a porosity from 10 to 90%, a thickness from 0.1 to 5 mm, and a capillary pressure air/water from (−1) to (−30) kPa. The transport barrier can have a porosity from 10 to 90%, a thickness in a direction of current between 0.05 and 5 mm, and a coefficient of permeability (in Darcy equation) from 1E-14 to 1E-10 m2. The alkali metal carbonate can have a total alkali metal (cation) concentration ranges from 0.1 to 10 molar. The alkali metal of the electrochemical reactor can comprise a cation selected from a group consisting of: sodium, potassium, rubidium and caesium, or a mixture thereof, and have a concentration in the range of 0.1 to 10 molar.
The electrochemical reactor can be a single-electrolyte flow chamber. The electrochemical reactor can further comprise an oxidation suppression barrier between the anode and the gas separation barrier that is composed of a porous electronically conductive and electrochemically inactive material. The electrochemical reactor can also comprise a porous electronically conductive connection plate and an O2 or CO2 selective membrane in adjacent contact with the product gas exit channel that serves to discharge O2 or CO2 gas from an O2 or CO2 gas exit channel.
Multiple electrochemical reactors can be combined into a stack. Discharged O2 or CO2 gas from a first electrochemical reactor in the stack can be fed to an adjacent second electrochemical reactor to depolarize a cathode of the second electrochemical reactor. In another electrochemical stack configuration, discharged gas stream comprising H2 from a first electrochemical reactor in the stack can be fed to an adjacent second electrochemical reactor to depolarize and prevent electro-oxidative destruction of an anode of the second electrochemical reactor.
According to another aspect of the invention, there is provided a method for removing CO2 from air comprising: contacting air with a regenerated absorbent in a CO2 absorber to produce a spent absorbent comprising carbonate in an alkali metal hydroxide and carbonate solution; feeding the spent absorbent to the aforementioned electrochemical reactor and producing an anode product stream comprising at least CO2 gas and an electrolyte product stream comprising alkali metal hydroxide and carbonate; and recycling the alkali metal hydroxide and carbonate from the electrolyte product stream into the regenerated absorbent for the CO2 absorber. The regenerated absorbent can be an aqueous solution comprising alkali metal hydroxide and carbonate; the electrolyte product stream can further comprise hydrogen and the method can further comprise separating the hydrogen from the electrolyte product stream and separating and recovering the CO2 gas from the anode product stream. The anode product stream can comprise O2 gas in which case the method further comprises separating the O2 gas from the anode product stream and discharging the O2 gas to atmosphere.
The method can further comprise supplying an electrical current to the electrochemical reactor to produce an average superficial current density on the anode in the range of 1 to 10 kA/m2 and an average current concentration in the porous anode in the range of 100 to 10,000 kA/m3.
The method can further comprise feeding the spent absorbent and the electrolyte product stream to a mixer for mixing into a mixed stream, which flows to a flow divider that divides the mixed stream respectively to the CO2 absorber as a regenerated absorbent stream and to the electrochemical reactor as an electrolyte feed stream. A feed rate of the electrolyte feed stream can be two to six times the feed rate of the regenerated absorbent stream. The alkali metal hydroxide and carbonate in the regenerated absorbent can have an [OH−]/[CO3=] ratio of in the range of 0.5 to 2.5 M/M, wherein the alkali metal hydroxide and carbonate in the produced electrolyte product stream has an [OH−]/[CO3=] ratio in a range of 1 to 6 M/M.
According to another aspect of the invention, there is provided a direct air capture (DAC) system comprising an electrochemical reactor for regenerating MOH and CO2 from M2CO3 when coupled to a power supply; and a CO2 absorber. The electrochemical reactor comprises a porous electronically conductive cathode having an inlet for receiving a pressurized electrolyte feed stream comprising MOH, M2CO3 and H2O, and an outlet for discharging an electrolyte product stream comprising MOH, M2CO3, H2O and H2; a porous electronically insulating hydrophilic transport barrier in adjacent contact with the cathode and configured to regulate the transport of electrolyte species and impede gas flow across the transport barrier; a porous electronically conductive hydrophilic anode in adjacent contact with the transport barrier and configured to generate CO2 in the presence of MOH while suppressing their recombination; a porous hydrophobic gas separation barrier in adjacent contact with the anode and configured to pass gases including CO2 and suppress liquids; and a product gas exit channel in adjacent contact with the gas separation barrier that serves to discharge an anode product stream comprising at least CO2 gas. The CO2 absorber comprises an alkali metal hydroxide and carbonate absorbent for contacting with air to produce a spent absorbent comprising carbonate in an alkali metal hydroxide and carbonate stream. The CO2 absorber further comprises an absorbent outlet fluidly coupled to the cathode inlet to supply the spent absorbent to the electrochemical reactor, and an absorber inlet fluidly coupled with the cathode outlet to receive the electrolyte product stream from the electrochemical reactor.
The DAC system can further comprise a mixer having inlets fluidly coupled to the absorbent outlet and the electrochemical reactor cathode outlet, wherein the spent absorbent stream and electrolyte product stream are mixed into a mixed stream; and a flow divider having an inlet fluidly coupled to the mixer to receive the mixed stream, and a pair of outlets for respectively discharging the mixed stream as a regenerated absorbent stream into the CO2 absorber and as the electrolyte feed stream into the electrochemical reactor.
The anode product stream can comprise O2 and CO2 gases, in which case the DAC system can further comprise a CO2/O2 separator having an inlet fluidly coupled with the anode product stream and CO2 and O2 outlets for discharging CO2 and O2 gases respectively. The DAC system can further comprise an H2 separator having an inlet fluidly coupled to the cathode outlet for receiving the electrolyte product stream, an H2 outlet for discharging H2 gas separated from the electrolyte product stream, and an alkali metal hydroxide and carbonate outlet fluidly coupled to the absorber inlet for discharging a metal hydroxide and carbonate stream; and an oxidation reactor coupled with the electrochemical reactor product gas exit channel or to the CO2/O2 separator O2 outlet to receive the anode product stream or the O2 gas as oxidant, and fluidly coupled with the separator H2 outlet to receive the H2 gas as fuel.
According to another aspect of the invention, there is provided a DAC system comprising: an electrochemical reactor for regenerating MOH and CO2 from M2CO3 when coupled to a power supply, a CO2 absorber, and an oxidation reactor. The electrochemical reactor is a single-electrolyte flow chamber electrochemical reactor comprising: an electrolyte flow channel having an inlet for receiving an electrolyte feed stream comprising MOH, M2CO3 and H2O, and an outlet for discharging an electrolyte product stream comprising MOH, M2CO3, and H2O; a porous electronically insulating hydrophilic first transport barrier in adjacent contact with a first side of the electrolyte flow channel and configured to regulate the transport of electrolyte species and impede gas flow across the barrier; a porous electronically conductive hydrophilic cathode in adjacent contact with the first transport barrier; a porous hydrophobic H2 separation barrier in adjacent contact with the cathode and configured to pass gases including H2 and suppress liquids; a cathode gas exit channel in adjacent contact with the H2 separation barrier and for discharging a cathode gas stream comprising H2; a porous electronically insulating hydrophilic second transport barrier in adjacent contact with a second side of the electrolyte flow channel and configured to regulate the transport of electrolyte species and impede gas flow across the barrier; a porous electronically conductive hydrophilic anode in adjacent contact with the second transport barrier configured to generate CO2 in the presence of MOH while suppressing their recombination; a porous hydrophobic gas separation barrier in adjacent contact with the anode and configured to pass gases including CO2 and O2 and suppress liquids; and an anode gas exit channel in adjacent contact with the gas separation barrier and for discharging an anode product stream comprising at least O2 and CO2.
The CO2 absorber comprises an alkali metal hydroxide and carbonate absorbent for contacting with air to produce a spent absorbent stream. The CO2 absorber further comprises an absorber outlet fluid coupled with the electrolyte flow channel inlet to supply the spent absorbent stream into the electrolyte feed stream, and an absorber inlet fluidly coupled with the electrolyte flow channel outlet to receive the electrolyte product stream into the alkali metal hydroxide and carbonate absorbent. The oxidation reactor is coupled with the anode gas exit channel to receive the anode product stream as oxidant, and is fluidly coupled with the cathode gas exit channel to receive the cathode gas stream as fuel. The oxidation reactor can be, for example, a fuel cell or a gas burner.
Embodiments of the invention comprise an electrochemical reactor in which a carbonate containing electrolyte contacts a hydrophilic transport barrier (not an ion-exchange membrane) covering a porous anode backed by a hydrophobic gas separation barrier. In this context, “transport” includes convection, diffusion and ion migration which all contribute to the transfer of species between (to and from) the cathode and anode, “hydrophilic” means an air/water contact angle less than 90° and typically less than 10°, and “hydrophobic” means an air/water contact angle greater than 90° and typically greater than 1100. In operation of the reactor, an electrolyte solution penetrates the hydrophilic transport barrier to reach the anode where water is oxidised by Reaction 6:
H2O(l)→2H+(aq)+½O2(g)+2e− Reaction 6
The pH of the bulk electrolyte in the anode may be well above 6 but near the anode surface a pH below 6 can promote generation of CO2 by net Reaction 7, from which it may recombine with hydroxide in the thermochemical Reaction 8 (“near” means within about 100 microns of the anode surface, i.e. the “Nernst diffusion layer” at the solid/liquid interface):
CO3=(aq)+2H+(aq)→CO2(aq)+H2O(l)+CO2(g)+H2O(l) Reaction 7
CO2(aq,g)+2OH−(l)→CO3=(aq)+H2O(l) Reaction 8
Wherein CO2(aq,g) means CO2 in solution and/or the gas phase
Electrochemical reactors (a.k.a. “cells”) referred herein use three-dimensional (3D) electrodes and the current density (CD) is reported as the superficial current density. The superficial (a.k.a. “geometric”) CD is the ratio of current to electrode area averaged over the external surface of the electrode, not to be conflated with the lower “real” CD on the internal surface area of the electrode. The unit of CD used here is kiloAmpere per square meter=kA/m2
Where: 1 kA/m2=1000 A/m2=100 mA/cm2
Since it is determined by a sequence of electrochemical (Faradaic) and thermochemical reactions the efficiency of the electrochemical process is measured/represented here not as the Faradaic efficiency (FE) but as the “current efficiency” (CE) where:
CE=(amount of product)/(stoichiometric equivalent of electric charge consumed)
e.g. CE for hydroxide (OH−)=(moles OH− produced)/(Faradays of charge consumed)
The current efficiency for both CO2 and hydroxide in the overall process is expected to depend on the relative rates of reactions 6 to 8, together with the rates of mass transfer of CO2 between phases and of its escape from the anode via the hydrophobic barrier.
Without being bound by theory, it is expected that current efficiency would depend on the current density, current concentration and ease of CO2 disengagement from the anode. Current concentration is the ratio of current to the pore volume of the anode and can be estimated with Equation 1:
CC=CD/(et) Equation 1
Where:
Both the current density and current concentration may be involved because electrochemical and thermochemical reactions 6 and 7 generating protons and CO2 happen at or near the solid electrode surface while thermochemical reactions consuming CO2 occur in the volume of entrained fluids. The subsequent disengagement of CO2 from the anode would depend in part on factors affecting multiphase fluid motion in porous solids, such as the liquid properties and the porosity, pore size, and contact angle in the solid.
Other factors likely to affect reactor performance include:
Considering that the irreversible second order thermochemical Reaction 8 is known to be fast (k=2E4 m3/kmol·s at 20° C. with activation energy=45 kJ/mol), one may expect this method would not achieve a useful conversion of carbonate to hydroxide. On the contrary, it was discovered that in embodiments of the invention having certain materials and conditions, the carbonate conversion with the electrochemical reactor can match or exceed that obtained in the thermochemical DAC causticizing process.
Embodiments of the invention have particular application to DAC systems. The performance and cost of DAC systems depend on many factors, one of which is the composition of the recycling alkaline absorbent. The usual absorbent is a solution of alkali metal hydroxide and carbonate in water. The alkali metal cation may be sodium (Na+), potassium (K+) or potentially caesium (Cs+). Lithium and rubidium are outliers here because Li2CO3 is relatively insoluble and Rb2CO3 relatively expensive. Potassium hydroxide and carbonate are more costly than corresponding sodium compounds but are preferred for their relatively high solubility in water and fast kinetics of the stepwise reactions 9 and 10 culminating in Reaction 8:
OH−+CO2→HCO3− Reaction 9
HCO3−+OH−→CO3═ Reaction 10
However sodium hydroxide/carbonate is satisfactory and even the more costly rubidium or caesium hydroxides/carbonates may be considered for applications requiring superior solubility, ionic strength and perhaps reactivity.
Regeneration of the alkaline absorbent by the causticizing Reaction 2 is critical to the thermochemical DAC process. Causticizing is a standard operation in the pulp and paper industry characterized by the conversion of carbonate to hydroxide, called the “causticizing efficiency” which ranges from about 70-90%. The causticizing efficiency relates to the equilibrium conversion in Reaction 2 and rests on the hydroxide/carbonate concentration ratio [OH−]/[CO3=], such as disclosed by Figuieredo L. et al., Semi-empirical modeling of the stationary state of a real caustizing system in a pulp mill”, Latin American Appl Research, 2012, 42, 319-326. Apart from the thermodynamic constraint on the [OH−]/[CO3=] ratio the thermochemical causticizing efficiency is restricted by reaction kinetics, as well as the presence of impurities affecting the morphology and subsequent thermal decomposition of calcium carbonate. Consequently, the design and optimization of the integrated thermochemical DAC system must consider the causticizing process, implicating the total alkali metal concentration [M+] and the [OH−]/[CO3=] causticizing ratio, which together fix the carbonate conversion and absorbent hydroxide concentration [OH−] via Equations 2 and 3:
X=(Rf−Ri)/(2+Rf) Equation 2
[OH−]=RY/(2+R) Equation 3
Where:
For example, U.S. Pat. No. 9,637,393 describe a fluidized pellet bed causticizing reactor with hydroxide and carbonate concentrations ranging respectively from 0.5 to 1.5 M and 0.2 to 0.9 M, corresponding to [OH−]/[CO3=] ratios from about 2.5 to 1.7 M/M and a carbonate conversion up to about 40%. The related DAC work of Keith et al. A process for capturing CO2 from the atmosphere, Joule 2 2018, 1573-1594 indicates KOH and K2CO3 concentrations ranging respectively from about 0.7-1.1 M and 0.5-0.7 M with a total [K+] near 2 M, [OH−]/[CO3=] from about 2.4 to 1.0 and corresponding carbonate conversion in Reaction 2 about 30%.
According to Stolaroff Carbon dioxide capture from atmospheric air using sodium hydroxide spray, Environ Sc & Tech 2008, 42(8), 2728-2735 and Mazzotti Direct air capture of CO2 with chemicals: Optimization of a two-loop carbonate system using a counter-current air-liquid contactor, Climate Change 2013, 18, 119-135, the size and cost of a CO2 absorber in DAC depends largely on the rate of absorption of CO2 into the alkaline absorbent, which is governed by the combined effects of CO2 gas-liquid mass transfer and the rate of Reactions 9/10. Mass transfer rates involve fluid-dynamic effects dependent on the diffusivity of CO2 together with the density, viscosity and surface tension of the absorbent solution. The more important kinetics of Reactions 9/10 are reported by Pohoreck, Kinetics of reaction between carbon dioxide and hydroxyl ions in aqueous electrolyte solutions, Chem. Eng Sci. 1988, 43(7), 1677-1684 to be controlled by Reaction 9 with an activation energy of about 45 kJ/mol and second order rate constant at 20° C. ranging from about [1-3] E4 m3/kmol·s, dependent on the ionic strength of the solution, as given by the simplified Equation 4:
Log[k/k*]=bl Equation 4
Where:
The NaOH/Na2CO3 and KOH/K2CO3 solutions reported by Pohoreck, of ionic strength=1 to 5 M′, correspond approximately to the composition of DAC absorbents, with the implication that the rate of CO2 absorption in DAC increases with ionic strength of the absorbent. This information on kinetics is relevant to embodiments of the present invention because it points to the [OH−]/[CO3=] ratio and total cation concentration [M+] with the coupled hydroxide concentration [OH−] as variables in the design and optimization of the DAC process.
Referring now to
Referring to
As will be described in detail below, the electrochemical reactor 10 can match the DAC absorbent compositions and allow their manipulation to optimize the overall DAC process.
Referring now to
Although there is electrolyte in both the cathode and anode, the electrochemical reactor can be considered to have a single-electrolyte flow chamber, since only one electrolyte solution enters, flows through and leaves the reactor via a single chamber, which may be the cathode 22 of the first and second embodiments (
For large scale operations such single cell, single-electrolyte flow chamber reactors, each with one anode-cathode pair, can be assembled in multi-cell stacks to operate in mono or bipolar mode with inter-cell fluid flows in parallel or in series.
The cathode and anode feeders 21, 27 are composed of an electronically conductive material such as stainless steel, graphite, nickel, or titanium. The cathode 22 has a porous three-dimensional structure and can for example be comprised of multiple layers of expanded nickel mesh. The porous hydrophilic transport barrier 23 serves to modulate transport to/from the anode 24 by convection, diffusion and ion migration and can comprise an electronically non-conductive microporous hydrophilic material such as hydrophilic polypropylene (e.g. SciMAT™, Vilidon™, Celgard™), borosilicate glass, asbestos, PES (polyethersuphone), hydrophilic PTFE, Zircar™ (zirconium oxide cloth) or Zirfon Perl™ (zirconium oxide in a polymer matrix); the material is an electronic insulator, made ionically conductive by absorbed electrolyte. The hydrophilic transport barrier 23 can have an air/water capillary pressure at least 1 kPa at 20° C., to impede anode gases from “backing up” into the cathode 22 and vice versa, and a permeability chosen to suppress/regulate the transport of electrolyte into the anode 24.
A limited transport (including convection, diffusion and migration) of electrolyte, water and/or ions into the anode 24 is needed to sustain the anode reactions. Such transport can be partly regulated by the permeability and thickness of the transport barrier 23, and the pressure difference between the cathode 22 and anode 24, as given in the Darcy equation—Equation 5:
Q=−(KA/u)(dP/(dL) Equation 5
Where:
The thickness and permeability of the transport barrier 23 is chosen to balance its ionic resistance with its role in regulating mass transport between cathode and anode. The barrier can comprise single or multiple layers with total thickness from about 0.05 and 5 mm and more particularly from 0.1 to 5 mm, a porosity from 10 to 90% and an effective coefficient of permeability about 1E-10 to 1E-14 m2.
The anode 24 has a porous three-dimensional structure and can comprise an electronically conductive fine mesh, felt, sintered fibre/particulate or foam of resistant material such as titanium or Ebonex (Ti407), with a catalytic surface for electro-oxidation of water at a pH below 12, such as ruthenium/iridium oxide, platinum, Ti4O7 or boron-doped diamond. The anode 24 may have a range of capillary properties but preferably a positive air/water capillary pressure to maintain contact with the aqueous electrolyte and suppress CO2 gas back-up into the cathode 22. In some embodiments, the anode 24 can have a porosity from 10 and 90%, a pore size from 10 to 1000 micron, a thickness of 0.2 to 20 mm, a specific surface area at least about 5000 m−1, an air/water wetting angle from 0 to 89° and an air/water capillary pressure at or above 1 kPa.
The porous hydrophobic [CO2+O2] gas separation barrier 25 serves to disengage carbon dioxide and oxygen gas from the hydroxide/carbonate electrolyte in the anode 24, and can comprise an electronically conductive or non-conductive microporous hydrophobic material, such as: a highly Teflonated (e.g. 50 wt % PTFE) gas transport layer (e.g. Spectracarb, Toray and other carbon papers known in the art), or a fine metal foam (e.g. nickel, titanium with >50 pores per inch) coated with a hydrophobic material like PTFE, or alternatively a microporous hydrophobic material such as PTFE alone. The [CO2+O2] gas separation barrier 25 may be composed of an electronic conductor or insulator material. An electronic conductor material is preferred but if the [CO2+O2] gas separation barrier 25 is composed of an electronically non-conductive material, an electronic connecter (not shown) is provided to electronically connect the anode feeder 27 and anode 24. The [CO2+O2] gas separation barrier 25 should have a high contact (wetting) angle and negative capillary pressure with water (preferably greater than about 100° and more negative than about −5 kPa) to stop/suppress electrolyte liquid transport from the anode 24 into the product gas exit stream 26, and may be treated with a super-hydrophobic substance such as one of the fluorinated organic compounds sold under the trade-name Cytonix™ (e.g. Cytonix PFC602A). A high selectivity (preferably above 99%) of gas vs. liquid is desired for 25 to prevent losses of hydroxide and CO2 in the process. In some embodiments, the gas separation barrier 25 can have a porosity from 10 to 90%, a thickness from 0.1 to 5 mm, and a capillary pressure air/water from (−1) to (−30) kPa.
Capillary pressure in this case is the pressure required for a liquid to penetrate a porous material and is estimated by the Young-Laplace (Equation 6):
P=2Y cos θ/r Equation 6
Where:
The contact angle of liquid water against air on a hydrophobic solid exceeds 90° so the capillary pressure has a negative value, the absolute value of which is effectively the pressure required to force liquid into/through the pores of the solid, known as the “breakthrough pressure”. With hydrophilic solids the contact angle is below 90° and the positive water/air capillary pressure is effectively the pressure required to force air (gas) into/through the liquid saturated pores, which is the “bubble-point” of a porous membrane.
In one example, the electrochemical reactor 10 has a “zero-gap” single-electrolyte chamber cell wherein the micro-porous hydrophilic transport barrier 23 is alkali resistant with a thickness about 0.1 to 1 mm, and bubble-point above about 2 kPa the anode 24 is porous and hydrophilic with a thickness about 1 to 10 mm and a specific surface area at least about 5000 m−1, and the hydrophobic gas separation barrier 25 is micro-porous and has thickness of about 0.1 to 2 mm and breakthrough pressure above about 2 kPa (absolute value).
In operation, the electrochemical reactor 10 generates MOH and CO2 from the electrolyte feed stream 30 according to the electrochemical process:
M2CO3+2H2O---2e−→2MOH+CO2+H2+0.5O2 Reaction 11
wherein the reaction at the cathode 22 is:
2H2O+2e−→2OH−+H2 Reaction 12
and the net reaction at the anode 24 is:
CO3=→CO2+0.5O2+2e− Reaction 13
Pressure differentials across the cathode 22, transport barrier 23, anode 24, [CO2+O2] gas separation barrier 25, and product gas exit channel 26 under operating conditions should be maintained to effect the desired phase separations while accommodating the thickness, porosity, pore size, permeability and surface properties of these components 22, 23, 24, 25, 26. The electrolyte space velocity (a.k.a. flow) is set through the material balance to match the reaction stoichiometry(s) and carbonate conversion.
Without being bound by theory, it is supposed that when current flows from the power supply, carbonate, hydroxide, water and cations are transported from the electrolyte in the cathode 22, across the porous hydrophilic transport barrier 23, and into the anode 24 where they are involved in a sequence of electrochemical and thermochemical reactions. The electrochemical Reaction 14 oxidizes water to generate protons (H+), while the thermochemical Reaction (15), which is favored by increased temperature, produce liquid H2O and gaseous CO2.
H2O→2H++0.5O2+2e− Reaction 14
2H++CO3−=→H2CO3(aqueous)→CO2(gas)+H2O(liq) Reaction 15
The hydrophobic [CO2+O2] gas separation barrier 25 allows the passage of CO2 and O2 to the product gas exit channel 26 but prevents electrolyte solution (with carbonate and hydroxide) from leaking through into the product gas exit channel 26 and recombining with the product CO2.
The anode 24 generates CO2 in the presence of hydroxide while suppressing their recombination. The distribution and relative rates of reactions and processes are arranged to suppress the generated CO2 from reacting with the hydroxide at the anode surface to reproduce carbonate (undesirable), and to encourage CO2 disengagement from the anolyte/anode and passage through the hydrophobic [CO2+O2] gas separation barrier 25 and to the product gas exit channel 26 (desirable). The distribution and rates of the electrochemical reaction(s) in the anode 24 depend on the superficial current density, current concentration and electronic & ionic conductivities of the anode and electrolyte, as well as the anode catalyst, specific surface, porosity and pore size distribution. The rate of the thermochemical reactions in the electrolyte depends on the reactant concentrations, temperature and the volume of electrolyte in and around the anode 24 (a.k.a. the electrolyte hold-up) which in turn depends on the thickness, porosity and wettabilities of the hydrophilic transport barrier 23 and the anode 24, as well as any extraneous fluid volume between the hydrophilic transport barrier 23 and the [CO2+O2] gas separation barrier 25 in which CO2 may recombine with the electrolyte by Reaction 8.
It is theorized that CO2 recovery can be increased by increasing the superficial current density and/or current concentration, decreasing the electrolyte hold-up in the hydrophilic transport barrier 23, anode 24 and [CO2+O2] gas separation barrier 25, promoting fast disengagement of the gas from the anode 24 into the [CO2+O2] gas separation barrier 25 and preventing electrolyte leakage through the [CO2+O2] gas separation barrier 25. It is proposed that gas disengagement may be assisted by constructing the porous anode with a biphilic morphology that allows in-situ partitioning of gas and liquid, for example with large (e.g. 100 um) hydrophilic pores coupled to small (e.g. 1 um) hydrophobic pores, wherein “biphilic” means having heterogeneous surfaces with spatially distinct regions of wettability including hydrophilic components. Correspondingly, this phase separation effect may be obtained with a stack of hydrophilic porous electrodes alternating with porous hydrophobic gas channels oriented parallel to the direction of current in the electrochemical reactor.
It is further supposed that performance of the single-chamber reactor 10 depends on the combined behaviour of the hydrophilic transport barrier 23, the anode 24 and the hydrophobic gas separation barrier 25, collectively referred to here as the “anode/separator assembly”. When the carbonate conversion exceeds zero the hydrophilic barrier 23 regulates the transport of hydroxide, carbonate and water from cathode to anode and prevents the flow of gas from cathode 22 to anode 24 and vice versa, while the hydrophobic barrier 25 prevents electrolyte leakage into the [CO2+O2] gas product 26-32. This reactant partitioning and phase separation is realized by the capillary properties of the barriers 23 and 25 and driven by pressure differences between the anode/separator assembly, the cathode 22 and the [CO2+O2] gas product 26. Improper control of the pressures may drive H2 gas into the anode 24 and/or CO2 gas into the cathode 22 and/or liquid electrolyte into the product gas chamber 26 with consequent loss of the process efficiency. Performance may also be affected by multi-phase fluid dynamics in the cathode 22, where the volumetric gas/liquid flow ratio can exceed 1 at high current density, with consequences for the effective conductivity of the electrolyte and pressure profile in the cathode.
The electro-active anode 24 has a key role in the generation and separation of the product gas 32. Under operating conditions the pH of bulk electrolyte in the anode is presumably between about 7 and 14 while the pH at/near the anode surface can be below about 6. In that case water is oxidised to protons on the anode surface by the electrochemical Reaction 14 followed by the conversion of carbonate to CO2 in the thermochemical Reaction 15, while CO2 may revert to carbonate/bicarbonate in the parallel thermochemical Reaction 8:
The disposition of the reactions depends on a number of factors known in the art to affect the potential and current distribution in 3D electrodes, for example: the anode electrocatalyst, electronic conductivity, thickness, porosity, pore size and pore surface contact angle, as well as the liquid hold-up and ionic conductivity of the electrolyte and the pressure and temperature dependent kinetics of the multiphase thermochemical reactions.
Apart from process dynamics, the practical long term (i.e. commercial) operation of the reactor must account for the electrode potential distribution through the anode which may result in electro-oxidizing conditions at the anode—hydrophobic barrier 24-25 interface. A consequent oxidation of the substrate (e.g. carbon, nickel) and/or hydrophobic constituents of the barrier (e.g. PTFE) can lower its (absolute) capillary pressure and allow electrolyte to pass into the [CO2+O2] gas product chamber 26. To prevent this undesired effect the anode 24 should be devised with an electrocatalyst, thickness, porosity and conductivity sufficient to keep the potential of the hydrophobic barrier 25 below a destructive value over the operating range of the reactor, particularly with superficial current densities above 1 kA/m2. Alternatively the hydrophobic barrier 25 can be protected against oxidation by a layer of porous electronically conductive but electrochemically inactive material, for example a “valve metal” such as titanium, tantalum, zirconium and niobium.
Trial and error experiments suggest that when Reaction 14 is driven at sufficiently high current density and/or current concentration and the liquid hold-up is sufficiently low then the relatively slow kinetics of Reaction 8 allow some CO2 to disengage from the anode without reverting to carbonate/bicarbonate. The fraction of CO2 disengaged being dependent in part on the hydroxide concentration driving Reaction 8 and hence on the total cation concentration [M+] and [OH−]/[CO3=] ratio, along with the corresponding carbonate conversion, as indicated in Equations 2 and 3. With suitable specification of components and operating conditions, the performance of the single-electrolyte chamber reactor 10 can be approximately matched with typical carbonate conversion and hydroxide regeneration regimes of DAC.
In some embodiments, the electrochemical reactor 10 is operated continuously at temperatures above 30° C. with a superficial current density in the range of 1 to 10 kA/m2 and in certain cases above about 2 kA/m2 and/or a current concentration in the range of 100 to 10,000 kA/m3 and in certain cases above about 500 kA/m3. Somewhat surprisingly, the hydroxide current efficiency of the electrochemical reactor 10 seems to increase with increasing current density and temperature, with operation at superficial current densities (e.g. about 2 to 10 kA/m2), well above those of the related prior art.
The operation of the electrochemical reactor 10 includes the co-production of hydrogen. The hydrogen to carbon dioxide ratio is estimated by Equation 7 and may be varied to suit downstream processes such as the conversion of CO2 to methanol (e.g. H2/CO2=3/1) or transportation fuels, as shown in
Referring to
In place of the anode feeder 27 in the first embodiment of the electrochemical reactor 10, the second embodiment of the electrochemical reactor 110 has a porous electron conductive connection plate 37 with an oxygen separation membrane 38 seated centrally within the electronically conductive connection plate 37. The O2 separation membrane 38 could be selective for O2 or for CO2, either of which could accomplish the desired separation. The porous electronically conductive plate 37 can be perforated with small holes (e.g. <2 mm) or comprise felted or sintered fibres or particles with a porosity of about 30 to 90%, 0.1 to 2 mm thick. The oxygen separation membrane 38 separates O2 from anode gas 34 of cell 32 and transfers it to cathode 36 of cell 33. The oxygen separation membrane can comprise a polymeric permeable material such as those currently under development for various gas separation applications, analogous to those disclosed by Han Y. et al., Polymeric membranes for CO2 separation and capture, J. Membrane Sci. 2021. The adjacent cell 33 comprises a porous cathode feeder 41 which allows O2 to pass from the product gas exit channel 26, through the oxygen separation membrane 38 and into the cathode 36 of the adjacent cell 33. The adjacent cell 33 also comprises a porous hydrophilic transport barrier 43 and the adjacent cathode 36 may be a gas diffusion electrode, trickle-bed or other 3D electrode suitable for reaction of gases with low solubility in water.
Referring now to
The electrochemical reactor 210 comprises a cathode feeder 221, a cathode gas (H2) exit channel 222, a porous hydrophobic H2 separation barrier 223, a cathode 224, a first porous hydrophilic transport barrier 225, an electrolyte flow channel 226, a second porous hydrophilic transport barrier 227, a porous hydrophilic anode 228, a porous hydrophobic [CO2+O2] gas separation barrier 229, a product gas exit channel 230, and an anode feeder 231. The electrolyte flow channel 226 has an inlet at one end to receive an electrolyte feed stream 30 comprising MOH, M2CO3 and H2O, and an outlet at another end to discharge an cathode product liquid stream 31 comprising MOH, M2CO3, and H2O. The product gas exit channel 230 has an outlet to discharge a product stream 32 comprising mixed CO2 and O2. Gaskets (not shown) are provided in between components to direct fluid flows and prevent leakage.
The electrochemical reactor 210 operates similarly to the first embodiment 10 to perform electrochemical and thermochemical reactions to produce a mixed CO2 and O2 product stream 32. Unlike the first embodiment, H2 is separated from the cathode product stream 31 by arranging the cathode 224 like the anode 24 of the first embodiment, i.e. by providing the first porous hydrophilic transport barrier 225, porous hydrophilic cathode 224 and porous hydrophobic gas (H2) separation barrier 223.
Alternatively (not shown), the cathode 224 and hydrophilic barrier 223 can be removed and the electrolyte flow channel 226 operated as a 3D cathode in electronic contact with the cathode feeder 221 to generate hydrogen gas which separates from the electrolyte and passes through the first porous hydrophobic barrier 223 into the cathode gas exit channel 222.
The electrochemical reactor 210 can be configured in a multi-cell bipolar mode to:
Referring to
Embodiments of the electrochemical reactor 10, 110, 210 can comprise multiple adjacent cells to form a multi-cell bipolar or monopolar reactor “stack” (not shown). Such an electrochemical reactor stack could operate at superficial current density above 2 kA/m2 to convert a solution of about [0.4 M MOH+1 M M2CO3] to a DAC absorbent mixture of about [1 M MOH+0.7 M M2CO3]. For example, a 20 cell bipolar reactor stack with 0.5 m2 electrodes, along with an external (cf.
Referring now to
Referring to
2H2+O2→2 H2O Reaction 16
The concentrated CO2 then passes by stream P to water separator 56 where water is recovered via stream Q into water storage unit 58, and CO2 passes to the thermochemical (or electrochemical) reactor 50 in stream R.
In a third option the [CO2+O2] of stream I passes via stream S to a thermochemical (TC) reactor (burner) 60 where the O2 is removed by combustion with a hydrocarbon fuel U and the CO2 formed passes in stream T to the water separator 56 and on via stream R to adjust the H2/CO2 ratio for the desired reaction(s) in the reactor 50.
Oxygen separated by the CO2/O2 separator 52 (stream V) may be used in many ways, including for example in oxy-fuel combustion and as medical oxygen. Preferably the separated oxygen may be released to the atmosphere to compensate for oxygen consumed in the combustion of fossil fuels as in exemplary Reaction 17. Here it should be noted that such combustion requires consumption of at least one kmol of oxygen (32 kg) per kmol of CO2 (44 kg) produced. The capture and sequestration of CO2 implies a corresponding net deficit of atmospheric oxygen that may not be replaced by the usual natural mechanisms in Earth's failing ecosystem.
CH4+2O2+CO2+2H2O Reaction 17
As well as enabling removal of CO2 from the air, the electrochemical regeneration of absorbent could have a vital role in replacing the atmospheric oxygen consumed in the formation of that CO2.
Of note, in all cases the [CO2+O2], H2, O2, CO2 and air product gases contain H2O gas due to evaporation of water from the absorbent and electrolyte. The continuous operation of all systems outlined in
Although the electrochemical reactors shown in
More broadly, the use of electrochemical reactors 10, 110, 210 for regeneration may open the DAC design space to include a wider range of absorbent compositions than accessible with thermochemical causticizing. The electrochemical process is not constrained by factors affecting Reaction 2 and can obtain [OH−]]/[CO3=] ratios up to at least 5, corresponding to about 70% conversion of carbonate to hydroxide, as evidenced by experimental data that are discussed in more detail under Examples. For instance,
These (and other) experimental data invoke reflection on operating the CO2 absorber with process conditions outside the range considered viable for the thermochemical DAC process. That possibility is reinforced by evidence that the rate of absorption of CO2 depends largely on the rate of Reaction 8, which increases with both hydroxide concentration and ionic strength of the absorbent [see Pohoreck, Stolaroff]. Calculations based on Pohoreck with the data of
Optimum design of an integrated thermochemical-electrochemical DAC plant would start from selection of its location and scale—both of which would depend on the availabilities and prices of water and fossil-free electricity as well as the method of CO2 disposal or utilization. From this basis the scale of the plant could range from about 1E-3 to 1E3 tonne CO2 per day in either intermittent or continuous operation. The optimization objectives could for example include minimizing the capital cost, operating cost, some combination of capital and operating costs, energy consumption or another desirable outcome such as the carbon footprint of the process. With such objective(s), the design could consider the interacting effects of at least the following factors:
Operation of a CO2 direct air capture process comprising a CO2 absorber integrated in a recycle loop with an electrochemical reactor, wherein an aqueous alkali metal hydroxide/carbonate solution functions as both carbon dioxide absorbent and reactor electrolyte, could be optimized by:
Optimization of a parallel operation of absorber and electrochemical reactor could comprise: setting the ratio of absorbent-electrolyte flows to the reactor and absorber in the range about 2 to 6.
The selection of values in these ranges may be executed in any sequence, suited to optimize operation of the multi-variable non-linear interactive system.
Referring to
The equipment shown in
Table 2 lists specifications of materials used in the experimental reactor, except for the endplates, bolts and gaskets.
External dimensions of the experimental reactor, including endplates: about 22 cm×6 cm×4 cm
Superficial electrode dimensions of both anode and cathode: about 10 cm by 2 cm
Superficial anode and cathode area: about 20 cm2=2E-3 m2 (each)
1e−10
1e−10
1= uncompressed, 2= vs. liquid water at 20° C. 3= liquid water vs. air at 20° C. (positive = hydrophilic, negative = hydrophobic)
The experimental reactor was used in continuous recycle operation in the horizontal position, anode facing up and electrolyte flow in the lengthwise (longest) direction. Experiments were carried out under ambient conditions (20° C., 1 bar(abs)) without control of the reactor temperature. In some cases Joule heating took the reactor outlet temperature up to about 70° C. but in most runs the temperature ranged from about 20 to 40° C.
An experiment was conducted using an experimental reactor configured according to the embodiment shown in
All components were pressed tightly together between % inch Plexiglass endplates, held with eight insulated ¼ inch stainless steel bolts, with provision for electrical connection of the electrode feeders Items 1 and 7 to the DC power supply Sinometer RXN 1520D (not shown).
All components had inlet and/or outlet fittings/ports and are appropriately gasketed to direct the fluid flows and prevent leakage. The endplates, electric connections, fittings/ports, bolts and gaskets are not shown in the Figures.
Conditions
Initial electrolyte: 0.8 mole/litre (M) sodium carbonate (Na2CO3) in water. Total volume=1 litre
Electrolyte flow, lengthwise=20 ml/minute (recycling).
Current=1.8 to 5.4 Ampere DC. Operating time=22 hours.
Superficial current density (CD)=0.9 to 2.7 kA/m2
Temperature 20 to 50° C.
Pressure in electrolyte channel=approx 120 kPa(abs)
Pressure in anode gas out channel=approx 110 kPa(abs)
Anode gas flow (CO2(g)+O2(g)+H2O(g)) approx 20 to 40 standard millilitre/minute.
Periodic samples of electrolyte were taken throughout the batch recycle run and analysed for hydroxide [OH−] and carbonate [CO3=] concentration by sequential titration with phenolphthalein and methyl orange indicators. The corresponding integral current efficiencies for hydroxide were calculated as:
CE={([OH−]V)final−([OH−]V)initial}/(C/F) Equation 8
Where:
NB. The voltages recorded in all Examples are the “full cell” reactor voltages measured between the anode to cathode feeders, which include all components of the overall voltage balance well known in the art, except those in the current delivery lines and contacts with the SS feeder electrodes. Experimental observations indicated an internal loss of about 2 V at 6 kA/m2 due mostly to electronic contact resistance between components.
The chart in
An electrochemical reactor was assembled as in Example 1, except:
Hydrophilic barrier 23: glass fibre mat was replaced by 1 layer of Viledon microporous hydrophilic polypropylene, followed by a second SciMAT and a hydrophilic polymer felt, total barrier thickness 2.4 mm, pressed against the anode.
Porous hydrophilic anode 24: porous Ir/Ru/titanium anode replaced by TySAR platinised titanium fibre, uncompressed porosity 96%, thickness 3 mm.
Gas separation barrier 25: Spectracarb replaced by 1 layer of Teflonated nickel foam, 95 pore per inch, thickness 1.5 mm. Effective contact resistance under compression against stainless steel about 1 V at 2 kA/m2.
Results are shown in
An electrochemical reactor was assembled as in Example 1, except:
Hydrophilic barrier 23: SciMAT was replaced by 1 layer of borosilcate glass filter, thickness 0.3 mm, pore diameter 1 um, pressed against the anode.
Product gas exit channel 26: added one layer of TySAR platinised titanium fibre mat between gas separation barrier 25 and product gas exit channel 26 to prevent compression damage to the gas separation barrier 25.
Operating conditions and time were similar to those in Example 1, except the initial electrolyte held a mixture of 0.57 M hydroxide and 0.68 M carbonate, roughly equivalent to the spent DAC absorbent of ref 43 (Keith). The results are shown in
An electrochemical reactor was assembled as for Example 3, except:
Hydrophilic barrier 23: SciMAT was replaced by 1 layer of borosilicate glass filter, thickness 0.6 mm, pore diameter 3 um, permeability coefficient about 1E-12 m2.
Operating conditions were similar to those of Example 1, except the maximum superficial current density was increased to 4 kA/m2 and operating time reduced to 13 hours. The result of
In the operations of Examples 1, 2, 3, 4 the anode 24 was pressed directly onto the hydrophobic gas separation barrier 25. In those (and other) cases it was observed that with high current density (e.g. above 1 kA/m2) and long operating times (e.g. above 5 hours) the hydrophobic barrier lost effectiveness as it became increasingly hydrophilic and eventually was corroded and sometimes perforated along its edges. Since the anode was not depolarized by hydrogen (as in the prior art) the loss of effectiveness in the hydrophobic gas separation barrier 25 was assumed due to its electro-oxidation by the high anodic potential of contact with the anode 24.
In this Example, the electrochemical reactor was assembled as for Example 4, except:
Hydrophilic barrier 23: The glass filter was replaced by 1 layer of SciMAT and an approximately 0.2 mm thick titanium fibre felt (as in
Operating conditions were similar to those of Example 1, except the maximum superficial current density was increased to 7 kA/m2 while the rate of anode gas generation was observed over a period of 1 hour with the result of
An electrochemical reactor was assembled as in Example 5, except:
Cathode 22: Polypropylene mesh replaced by nickel foam, 1.6 mm thick, 150 um pores.
Hydrophilic barrier 23: Replaced by one layer of SciMAT plus 1 layer of Viledon hydrophilic polypropylene.
Hydrophobic gas separation barrier 25: Spectracarb 2050-1150 replaced by Toray carbon paper TGP-H-120 with 50% PTFE.
Operating conditions were similar to those of Example 5, except that the recycling electrolyte volume was reduced to about 0.5 litre and recycling electrolyte flow increased to about 100 ml/minute. A manometer (
The anode/cathode differential pressure was seen to affect performance of the reactor and consequently manipulated to some extent through the electrolyte flow rate, the height of the anode gas water column and a throttle on the electrolyte outlet—shown in the cathode out throttle 313 of the apparatus shown in
[OH−]=XY/(2+X) Equation 9
[CO3=]=Y/(2+X) Equation 10
Where: Y=[Na+] M, X=[OH−]/[CO3=] M/M
The [OH−]/[CO3=] ratio reported in this and subsequent Examples is more useful than the individual ion concentrations because it:
Starting from initial [OH−] and [CO3=] values of respectively 0.32 and 0.84 M the [OH−]/[CO3=] ratio increased from about 0.4 to 2.6 while [Na+] rose from about 2.0 to 2.3 M due to loss of water by evaporation and reaction. A high evaporative loss of water was due to continual air purge of the electrolyte feed tank. The superficial current density reached about 6 kA/m2 at 10 Volt (full cell) while integral hydroxide CE dropped from about 60 to 20%.
Examination of reactor components showed about 30% loss of hydrophobic area on gas separation barrier 25 together with black deposits on the transport barrier 23 and some loss of catalyst from the anode 24. These observations indicate a degree of corrosion of reactor components that may not be tolerable in a practical process. In subsequent experiments peripheries of the Ti felt between the anode 24 and transport barrier 23 were insulated to suppress high edge potentials suspected of corroding (i.e. oxidising) gas separation barrier 25. Note that this type of corrosion probably would not occur in prior art where the anode potential was kept low by depolarizing it with hydrogen.
Results of Examples 1 to 6 indicate that the reactor performance is affected by the thickness and permeability of the transport barrier 23 which would influence the rates of reactant transport to/from the anode as well as the reactor internal electric resistance.
An electrochemical reactor was assembled as in Example 6, except:
Anode 24: The porous Ir/Ru/Ti anode 25 was replaced by a platinised Ti fibre matrix (TySAR) with fibre diameter around 20 um and uncompressed porosity 96%, compressed in-situ from about 3.2 to 1.6 mm thickness to give porosity about 95%. The TySAR anode reactor was operated for 6 hours under conditions similar to Example 6 to give the result of
In a test similar to Example 7 the “uncompressed” TySAR was replaced by the same material firmly pre-compressed from 3.2 to 1.2 mm, porosity about 90%.
Examination of reactor components at this stage showed some loss of hydrophobicity on gas separation barrier 25, also although the hydrophilic polypropylene was stable in strong hydroxide. Hydrophilic transport barrier 23 slowly lost its wettability by contact with the anode at high current density. In experiments for Examples 9 to 12 the peripheries of the Ti felt (oxidation suppression barrier 5) were insulated to suppress high edge potentials suspected of corroding (i.e. oxidising) gas separation barrier 25 and a porous zirconium oxide textile (Zircar) was inserted between the hydrophilic transport barrier 23 and the anode 24. Zirconium oxide is highly hydrophilic and relatively stable to attack by hydroxide and oxidation in contact with the anode.
An electrochemical reactor was assembled as in Example 6, except:
Hydrophilic transport barrier 23: Became one layer of SciMAT plus 1 layer of Zircar ZYW 30A.
The reactor was operated for 10 hours with recycle electrolyte flow about 100 ml/minute, anode-cathode pressure difference about 0.8 kPa and superficial current density up to 9 kA/m2 to give the result shown in
Here it is notable that the [OH−]/[CO3=] ratio increases roughly step wise in concert with the current density—implying that current density affects the process selectivity according to the postulates in the Description.
An electrochemical reactor was assembled as in Example 9, except:
Hydrophilic transport barrier 23: became four layers: 1 SciMAT+1 PES membrane+1 SciMAT+1 Zircar ZYW 30A.
Operation was as for Example 9 except the electrolyte was 2 M potassium carbonate (K2CO3) and the superficial current density was held near 6 kA/m2 over 8 hours of operation, with an anode-cathode pressure difference about 2.7 kPa. The results of
An electrochemical reactor was assembled as in Example 9, except:
Hydrophilic transport barrier 23: became five layers: 2 SciMAT+1 PES membrane+1 SciMAT+1 Zircar ZYW 30A.
Anode 24: was changed to the parallel sandwich bi-philic configuration of
Operation over a period of 13 hours was as for Example 10 except the initial electrolyte was 1 M Na2CO3, flow about 50 ml/minute and superficial current density up to 4 kA/m2. The result of
An electrochemical reactor was assembled and operated as in Example 11, except the initial electrolyte was 3.3 M K2CO3 and the superficial current density reached about 5 kA/m2. The result of
Examination of the reactor components from Examples 9 to 12 showed relatively little effects from corrosion, presumably due to presence of the titanium felt oxidation suppression barrier 5 and Zircar cloth added to the reactor after Example 8.
Examples 9 to 12 show the electrochemical reactor can operate with sodium (Na) and with potassium (K) based absorbents/electrolytes and cation (Na+, K+) concentrations up to at least about 7 M, [OH−]/[CO3=] ratio up to at least about 5 and hydroxide concentration at least about 3 M. Depending on superficial current density the reactor voltage ranges from about 3 to 10 V while the integral CE for hydroxide hinges on the [OH−]/[CO3=] ratio and ranges from about 90 to 10%. The range of CE indicates the possibility of producing H2/CO2 mole ratios from about 2 to 6, suitable for the downstream production of fuels, etc.
The current and energy efficiencies, operating life, capital cost, operating cost, safety, location, etc. would be important aspects of using an electrochemical reactor/process in a DAC plant. These issues are not considered here, except to note that the experimental data come from apparatus not optimized with respect to materials/configuration/dimensions and operating conditions, nor tested in continuous operation over times longer than 24 hours. Nevertheless it is useful to consider
From the above description, examples and elaboration it will be apparent to those “skilled in the art” of process engineering that the electrochemical option offers several possibilities for design and optimization of the coupled absorption and regeneration steps in DAC that are not available in the conventional thermochemical system. However, CO2 absorption catalysts and impurities in the absorbent-electrolyte have not been tested in the electrochemical reactor and their presence in an “industrial” DAC process could affect the electrochemistry and challenge this conjecture.
Although
Note that “Electrochemical reactor” used here is generic and could mean a single cell (one anode/cathode pair), multiple single cells or a multi-cell stack operated in mono or bipolar mode, with fluid flows to reactors and cells in series or parallel.
Reactors may operate in the batch or continuous manner with fluids in plug flow, stirred or otherwise motivated.
Terms used here without explanation have common meanings in chemistry and engineering.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. Accordingly, as used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and “comprising,” when used in this specification, specify the presence of one or more stated features, integers, steps, operations, elements, and components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and groups. Directional terms such as “top”, “bottom”, “upwards”, “downwards”, “vertically”, and “laterally” are used in the following description for the purpose of providing relative reference only, and are not intended to suggest any limitations on how any article is to be positioned during use, or to be mounted in an assembly or relative to an environment. Additionally, the term “couple” and variants of it such as “coupled”, “couples”, and “coupling” as used in this description are intended to include indirect and direct connections unless otherwise indicated. For example, if a first device is coupled to a second device, that coupling may be through a direct connection or through an indirect connection via other devices and connections. Similarly, if the first device is communicatively coupled to the second device, communication may be through a direct connection or through an indirect connection via other devices and connections.
It is contemplated that any part of any aspect or embodiment discussed in this specification can be implemented or combined with any part of any other aspect or embodiment discussed in this specification.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CA2021/051159 | 8/20/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63069302 | Aug 2020 | US |
